FDA UDI In Commercial Distribution 🇺🇸 United States

Pro Nox

DI: 17540195040073 · Model: CMI-0100-PNX · O-Two Medical Technologies Inc
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Pro Nox
Primary DI
17540195040073
Version / Model
CMI-0100-PNX
Company Name
O-Two Medical Technologies Inc
Labeler DUNS
206449154
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-11-13
Public Version
1
Public Version Date
2023-11-21
Public Version Status
New
Public Device Record Key
6b5e7705-0b07-4e2b-9a8f-a1682b3387d9

Device Description

The PRO NOX Relieve Nitrous Oxide/Oxygen Analgesic Gas Mixing and Delivery System is a portable pneumatically powered device designed to provide a 50/50% nitrous oxide and oxygen mixture. It provides two input connectors for connection with nitrous oxide and oxygen cylinders through pressure regulators. The device has only one control for turning ON or OFF the device. When it is turned ON, the output of N2O/O2 gas mixture will only be activated by an inspiratory effort by the patient. The out put of N2O/O2 gas mixture is pre-set at 50/50%. Neither the patient nor medical personnel are able to adjust, eliminating the risk of delivering a hypoxic mixture.

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
BZR Mixer, Breathing Gases, Anesthesia Inhalation

GMDN Terms

Code Name
16953 Inhalational analgesia unit

Identifiers

Type ID
Primary 17540195040073
Direct Marking 07540195040076

Customer Contacts

Phone
9057926896

Premarket Submissions

Submission Number Supplement Number
K113687 000